← Return to Anyone been treated at Mayo Clinic for Ocular Myasthenia Gravis?

Discussion

Anyone been treated at Mayo Clinic for Ocular Myasthenia Gravis?

Autoimmune Diseases | Last Active: Sep 14 6:47am | Replies (35)
Comment receiving replies
@wcburns2

Thanks for your response. One of my appointments is for that ENG test. I am staying positive about learning something new but not expecting anything. I’ve not had that test yet.
Wishing you the best possible outcome.

Jump to this post

Replies to "Thanks for your response. One of my appointments is for that ENG test. I am staying..."
Laurie J Van Roekel | @laurievr | Jul 13 8:05pm

I was fully expecting the ENG test to confirm MG, but it did not. Blood tests did not confirm it, either. The Parkinson diagnosis was from the Mayo doctor in charge of all of my treatment/tests, and he observed some PD symptoms that I showed but wasn't aware of. I hope you will have the ENG test and get a result one way or another. Knowledge of what we are dealing with is so important. I wish you well in your testing.

VIEW AND REPLY